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European Journal of Cardio-Thoracic Surgery, Vol 5, 368-371, Copyright © 1991 by European Association for Cardio-thoracic Surgery
R Neirotti, A Nijveld, M Ithuralde, M Quaglio, C Seara, L Lubbers, J Schuller and R Mollen
From 1980 to 1990, 12 patients (mean age 2.5 years, range 5 months to 9
years) with anomalous origin of the left coronary artery from the pulmonary
artery were treated surgically. Five infants were operated upon in the
first year of life because of persistent symptoms of congestive heart
failure. In all cases, a two-coronary system was constructed by direct
aortic reimplantation of the anomalous vessel with no deaths early or late
over a follow-up period of up to 10 years. The technique of reimplantation
was facilitated by transection of the main pulmonary artery. One patient
with severe mitral regurgitation underwent, in addition, a mitral
annuloplasty. A pulmonary valvotomy was performed in another patient with
associated pulmonary stenosis. Three patients are receiving medication. The
reimplanted anomalous left coronary artery was patent in each reevaluated
patient (10/12). Left ventricular function improved considerably in all
cases. Patients with symptoms should undergo repair soon after diagnosis.
Direct aortic reimplantation should be technically feasible in even the
smallest infant. Operative mortality is related to preoperative conditions
and severity of ischemic damage of the myocardium.
ARTICLES
Anomalous origin of the left coronary artery from the pulmonary artery: repair by aortic reimplantation
Department of Pediatric Cardiac Surgery, Academical Medical Center, Amsterdam, The Netherlands.
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